Works matching DE "DELAYED puberty"


Results: 120
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    IGSF1 variants in boys with familial delayed puberty.

    Published in:
    European Journal of Pediatrics, 2015, v. 174, n. 5, p. 687, doi. 10.1007/s00431-014-2445-9
    By:
    • Joustra, Sjoerd;
    • Wehkalampi, Karoliina;
    • Oostdijk, Wilma;
    • Biermasz, Nienke;
    • Howard, Sasha;
    • Silander, Tanya;
    • Bernard, Daniel;
    • Wit, Jan;
    • Dunkel, Leo;
    • Losekoot, Monique
    Publication type:
    Article
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    Rare Causes of Primary Amenorrhea.

    Published in:
    Endokrinologiâ, 2019, n. 1, p. 36
    By:
    • Tsvetanova, Tsvetelina A.;
    • Kaleva, Nartsis N.;
    • Grozdanova, Liljana I;
    • Andonova, Silvija I.;
    • Linev, Alexandar J.;
    • Pehlivanov, Blagovest K.;
    • Matev, Magdalen G.;
    • Dimitrova, Diana G.
    Publication type:
    Article
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    A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2018, v. 10, n. 3, p. 206, doi. 10.4274/jcrpe.0032
    By:
    • Kardelen, Aslı Derya;
    • Toksoy, Güven;
    • Baş, Firdevs;
    • Abalı, Zehra Yavaş;
    • Gençay, Genco;
    • Poyrazoğlu, Şükran;
    • Bundak, Rüveyde;
    • Altunoğlu, Umut;
    • Avcı, Şahin;
    • Najaflı, Adam;
    • Uyguner, Oya;
    • Karaman, Birsen;
    • Başaran, Seher;
    • Darendeliler, Feyza
    Publication type:
    Article
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    Hypogonadotropic Hypogonadism due to Novel FGFR1 Mutations.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2017, v. 9, n. 2, p. 95, doi. 10.4274/jcrpe.3908
    By:
    • Akkuş, Gamze;
    • Kotan, Leman Damla;
    • Durmaz, Erdem;
    • Mengen, Eda;
    • Turan, İhsan;
    • Ulubay, Ayça;
    • Gürbüz, Fatih;
    • Yüksel, Bilgin;
    • Tetiker, Tamer;
    • Topaloğlu, A. Kemal
    Publication type:
    Article
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    Idiopathic Hypogonadotrophic Hypogonadism Caused by Inactivating Mutations in SRA1.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, p. 17
    By:
    • Ulubay, Ayça;
    • Kotan, L. Damla;
    • Cooper, Charlton;
    • Darcan, Şükran;
    • Carr, Ian M.;
    • Özen, Samim;
    • Yi Yan;
    • Hamedani, Mohammad K.;
    • Gürbüz, Fatih;
    • Mengen, Eda;
    • Turan, İhsan;
    • Akkuş, Gamze;
    • Yüksel, Bilgin;
    • Leygue, Etienne;
    • Topaloğlu, A. Kemal
    Publication type:
    Article
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    Idiopathic Hypogonadotropic Hypogonadism Caused by Inactivating Mutations in SRA1.

    Published in:
    Journal of Clinical Research in Pediatric Endocrinology, 2016, v. 8, n. 2, p. 125, doi. 10.4274/jcrpe.3248
    By:
    • Kotan, Leman Damla;
    • Cooper, Charlton;
    • Darcan, Şükran;
    • Carr, Ian M.;
    • Özen, Samim;
    • Yi Yan;
    • Hamedani, Mohammad K.;
    • Gürbüz, Fatih;
    • Mengen, Eda;
    • Turan, İhsan;
    • Ulubay, Ayça;
    • Akkuş, Gamze;
    • Yüksel, Bilgin;
    • Kemal Topaloğlu, A.;
    • Leygue, Etienne
    Publication type:
    Article
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